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Intestinal microbial communities associated with acute enteric infections and disease recovery
BACKGROUND: The intestinal microbiome represents a complex network of microbes that are important for human health and preventing pathogen invasion. Studies that examine differences in intestinal microbial communities across individuals with and without enteric infections are useful for identifying...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579588/ https://www.ncbi.nlm.nih.gov/pubmed/26395244 http://dx.doi.org/10.1186/s40168-015-0109-2 |
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author | Singh, Pallavi Teal, Tracy K. Marsh, Terence L. Tiedje, James M. Mosci, Rebekah Jernigan, Katherine Zell, Angela Newton, Duane W. Salimnia, Hossein Lephart, Paul Sundin, Daniel Khalife, Walid Britton, Robert A. Rudrik, James T. Manning, Shannon D. |
author_facet | Singh, Pallavi Teal, Tracy K. Marsh, Terence L. Tiedje, James M. Mosci, Rebekah Jernigan, Katherine Zell, Angela Newton, Duane W. Salimnia, Hossein Lephart, Paul Sundin, Daniel Khalife, Walid Britton, Robert A. Rudrik, James T. Manning, Shannon D. |
author_sort | Singh, Pallavi |
collection | PubMed |
description | BACKGROUND: The intestinal microbiome represents a complex network of microbes that are important for human health and preventing pathogen invasion. Studies that examine differences in intestinal microbial communities across individuals with and without enteric infections are useful for identifying microbes that support or impede intestinal health. RESULTS: 16S rRNA gene sequencing was conducted on stool DNA from patients with enteric infections (n = 200) and 75 healthy family members to identify differences in intestinal community composition. Stools from 13 patients were also examined post-infection to better understand how intestinal communities recover. Patient communities had lower species richness, evenness, and diversity versus uninfected communities, while principle coordinate analysis demonstrated close clustering of uninfected communities, but not the patient communities, irrespective of age, gender, and race. Differences in community composition between patients and family members were mostly due to variation in the abundance of phyla Proteobacteria, Bacteroidetes, and Firmicutes. Patient communities had significantly more Proteobacteria representing genus Escherichia relative to uninfected communities, which were dominated by Bacteroides. Intestinal communities from patients with bloody diarrhea clustered together in the neighbor-joining phylogeny, while communities from 13 patients’ post-infection had a significant increase in Bacteroidetes and Firmicutes and clustered together with uninfected communities. CONCLUSIONS: These data demonstrate that the intestinal communities in patients with enteric bacterial infections get altered in similar ways. Furthermore, preventing an increase in Escherichia abundance may be an important consideration for future prevention strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0109-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4579588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45795882015-09-24 Intestinal microbial communities associated with acute enteric infections and disease recovery Singh, Pallavi Teal, Tracy K. Marsh, Terence L. Tiedje, James M. Mosci, Rebekah Jernigan, Katherine Zell, Angela Newton, Duane W. Salimnia, Hossein Lephart, Paul Sundin, Daniel Khalife, Walid Britton, Robert A. Rudrik, James T. Manning, Shannon D. Microbiome Research BACKGROUND: The intestinal microbiome represents a complex network of microbes that are important for human health and preventing pathogen invasion. Studies that examine differences in intestinal microbial communities across individuals with and without enteric infections are useful for identifying microbes that support or impede intestinal health. RESULTS: 16S rRNA gene sequencing was conducted on stool DNA from patients with enteric infections (n = 200) and 75 healthy family members to identify differences in intestinal community composition. Stools from 13 patients were also examined post-infection to better understand how intestinal communities recover. Patient communities had lower species richness, evenness, and diversity versus uninfected communities, while principle coordinate analysis demonstrated close clustering of uninfected communities, but not the patient communities, irrespective of age, gender, and race. Differences in community composition between patients and family members were mostly due to variation in the abundance of phyla Proteobacteria, Bacteroidetes, and Firmicutes. Patient communities had significantly more Proteobacteria representing genus Escherichia relative to uninfected communities, which were dominated by Bacteroides. Intestinal communities from patients with bloody diarrhea clustered together in the neighbor-joining phylogeny, while communities from 13 patients’ post-infection had a significant increase in Bacteroidetes and Firmicutes and clustered together with uninfected communities. CONCLUSIONS: These data demonstrate that the intestinal communities in patients with enteric bacterial infections get altered in similar ways. Furthermore, preventing an increase in Escherichia abundance may be an important consideration for future prevention strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0109-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-22 /pmc/articles/PMC4579588/ /pubmed/26395244 http://dx.doi.org/10.1186/s40168-015-0109-2 Text en © Singh et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Singh, Pallavi Teal, Tracy K. Marsh, Terence L. Tiedje, James M. Mosci, Rebekah Jernigan, Katherine Zell, Angela Newton, Duane W. Salimnia, Hossein Lephart, Paul Sundin, Daniel Khalife, Walid Britton, Robert A. Rudrik, James T. Manning, Shannon D. Intestinal microbial communities associated with acute enteric infections and disease recovery |
title | Intestinal microbial communities associated with acute enteric infections and disease recovery |
title_full | Intestinal microbial communities associated with acute enteric infections and disease recovery |
title_fullStr | Intestinal microbial communities associated with acute enteric infections and disease recovery |
title_full_unstemmed | Intestinal microbial communities associated with acute enteric infections and disease recovery |
title_short | Intestinal microbial communities associated with acute enteric infections and disease recovery |
title_sort | intestinal microbial communities associated with acute enteric infections and disease recovery |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579588/ https://www.ncbi.nlm.nih.gov/pubmed/26395244 http://dx.doi.org/10.1186/s40168-015-0109-2 |
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